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ATPase H+ transporting accessory protein 2
Summary
- Gene Symbol
-
- ATP6AP2
- Aliases
-
- APT6M8-9
- ATP6M8-9
- M8-9
- PRR
- RENR
- V-ATPase M8.9 subunit
- prorenin receptor
- renin receptor
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Cell projection
- Cleavage on pair of basic residues
- Congenital disorder of glycosylation
- Cytoplasmic vesicle
- Disease variant
- Endoplasmic reticulum
- Endosome
- Epilepsy
- Intellectual disability
- Lysosome
- Neurodegeneration
- Parkinsonism
- Phosphoprotein
- Postsynaptic cell membrane
- Receptor
- Reference proteome
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| O75787 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| Golgi lumen acidification |
|
|
| synaptic vesicle lumen acidification | ||
| central nervous system maturation | ||
| head morphogenesis | ||
| angiotensin maturation |
GO Hierarchy
biological process
metabolic process [inference]
homeostatic process [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
regulation of biosynthetic process [inference]
positive regulation of metabolic process [inference]
regulation of cellular metabolic process [inference]
regulation of macromolecule metabolic process [inference]
positive regulation of biological process [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| autophagosome membrane | ||
| clathrin-coated vesicle membrane | ||
| vacuolar proton-transporting V-type ATPase, V0 domain | ||
| external side of plasma membrane | ||
| axon |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| signaling receptor activity | ||
| protein binding |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:4090 | agnosia | |
| DOID:417 | autoimmune disease | |
| DOID:4188 | echolalia | |
| DOID:4448 | macular degeneration | |
| DOID:445 | Bartter disease | |
| DOID:446 | primary hyperaldosteronism | |
| DOID:4676 | uremia | |
| DOID:4766 | embryoma | |
| DOID:483 | cavernous hemangioma | |
| DOID:4903 | granular cell carcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001848 | Calcaneovalgus deformity |
| HP:0002059 | Cerebral atrophy |
| HP:0002063 | Rigidity |
| HP:0002067 | Bradykinesia |
| HP:0002069 | Bilateral tonic-clonic seizure |
| HP:0002079 | Hypoplasia of the corpus callosum |
| HP:0002186 | Apraxia |
| HP:0002188 | Delayed CNS myelination |
| HP:0002240 | Hepatomegaly |
| HP:0002307 | Drooling |
| Disease ID | Disease Name |
|---|---|
| ORPHA:363654 |
|
| OMIM:300911 |
|
| OMIM:301045 |
|
| OMIM:300423 |
|
| ORPHA:93952 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 101046482 | SAIBB06994 | ||
| 101969955 | ICTTR14593 | ||
| 117026216 | RHIFE17799 | ||
| 100226045 | TAEGU11917 | ||
| 101810643 | FICAL09623 | ||
| 103231813 | CHLSB18381 | ||
| 108535862 | RHIBE37548 | ||
| 104662194 | RHIRO24463 | ||
| 100582064 | NOMLE38945 | ||
| 114596164 | PODMU19816 |
